Helga E.M. Malingré

Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of β-oxidation in insulin secretion

Peter T. Clayton, Simon Eaton, A Aynsley‐Green et al. · Journal of Clinical Investigation · 2001 · 253 citations

Metabolic Disorder, Human Growth, Pathology +22

Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of β-oxidation in insulin secretion

Peter T. Clayton, Simon Eaton, A Aynsley‐Green et al. · Journal of Clinical Investigation · 2001 · 252 citations · Full text

Human copper transporter 2 is localized in late endosomes and lysosomes and facilitates cellular copper uptake

Peter V. E. van den Berghe, Dineke E. Folmer, Helga E.M. Malingré et al. · Biochemical Journal · 2007 · 210 citations · Full text

Molecular Characterization of 3-Phosphoglycerate Dehydrogenase Deficiency—a Neurometabolic Disorder Associated with Reduced L-Serine Biosynthesis

Leo W. J. Klomp, Tom J. de Koning, Helga E.M. Malingré et al. · The American Journal of Human Genetics · 2000 · 109 citations · Full text

Reduced L-serine Biosynthesis, Molecular Characterization, Aldehyde Dehydrogenase +6

Human Short-Chain L-3-Hydroxyacyl-CoA Dehydrogenase: Cloning and Characterization of the Coding Sequence

Patrick J.C.M. Vredendaal, Inge E.T. van den Berg, Helga E.M. Malingré et al. · Biochemical and Biophysical Research Communications · 1996 · 56 citations

Biosynthesis, Aldehyde Dehydrogenase, Cellular Enzymology +11